Leite Montalvão Ana Paula, Kersten Birgit, Fladung Matthias, Müller Niels Andreas
Thünen Institute of Forest Genetics, Großhansdorf, Germany.
Front Plant Sci. 2021 Jan 15;11:580488. doi: 10.3389/fpls.2020.580488. eCollection 2020.
The diversity of inflorescences among flowering plants is captivating. Such charm is not only due to the variety of sizes, shapes, colors, and flowers displayed, but also to the range of reproductive systems. For instance, hermaphrodites occur abundantly throughout the plant kingdom with both stamens and carpels within the same flower. Nevertheless, 10% of flowering plants have separate unisexual flowers, either in different locations of the same individual (monoecy) or on different individuals (dioecy). Despite their rarity, dioecious plants provide an excellent opportunity to investigate the mechanisms involved in sex expression and the evolution of sex-determining regions (SDRs) and sex chromosomes. The SDRs and the evolution of dioecy have been studied in many species ranging from Ginkgo to important fruit crops. Some of these studies, for example in asparagus or kiwifruit, identified two sex-determining genes within the non-recombining SDR and may thus be consistent with the classical model for the evolution of dioecy from hermaphroditism via gynodioecy, that predicts two successive mutations, the first one affecting male and the second one female function, becoming linked in a region of suppressed recombination. On the other hand, aided by genome sequencing and gene editing, single factor sex determination has emerged in other species, such as persimmon or poplar. Despite the diversity of sex-determining mechanisms, a tentative comparative analysis of the known sex-determining genes and candidates in different species suggests that similar genes and pathways may be employed repeatedly for the evolution of dioecy. The cytokinin signaling pathway appears important for sex determination in several species regardless of the underlying genetic system. Additionally, tapetum-related genes often seem to act as male-promoting factors when sex is determined via two genes. We present a unified model that synthesizes the genetic networks of sex determination in monoecious and dioecious plants and will support the generation of hypothesis regarding candidate sex determinants in future studies.
开花植物花序的多样性引人入胜。这种魅力不仅源于所展示的大小、形状、颜色和花朵的多样性,还源于生殖系统的范围。例如,雌雄同体在植物界中大量存在,同一朵花中既有雄蕊又有雌蕊。然而,10%的开花植物有单独的单性花,要么在同一个体的不同位置(雌雄同株),要么在不同个体上(雌雄异株)。尽管雌雄异株植物很罕见,但它们为研究性别表达机制以及性别决定区域(SDRs)和性染色体的进化提供了绝佳机会。从银杏到重要的水果作物等许多物种都对SDRs和雌雄异株的进化进行了研究。其中一些研究,例如在芦笋或猕猴桃中,在非重组SDR内鉴定出两个性别决定基因,因此可能与从雌雄同体通过雌全异株进化为雌雄异株的经典模型一致,该模型预测有两个连续的突变,第一个影响雄性功能,第二个影响雌性功能,在一个抑制重组的区域中连锁。另一方面,在基因组测序和基因编辑的帮助下,其他物种出现了单因素性别决定,如柿子或杨树。尽管性别决定机制多种多样,但对不同物种中已知的性别决定基因和候选基因进行的初步比较分析表明,类似的基因和途径可能会在雌雄异株的进化中反复被采用。无论潜在的遗传系统如何,细胞分裂素信号通路在几个物种的性别决定中似乎都很重要。此外,当通过两个基因决定性别时,绒毡层相关基因似乎常常充当促进雄性的因子。我们提出了一个统一的模型,该模型综合了雌雄同株和雌雄异株植物性别决定的遗传网络,并将支持未来研究中关于候选性别决定因素的假设的产生。